| 摘要 |
<p>A method of organic synthesis comprising the protection of a hydroxy function characterized in that a 1-N-substituted-4-alkoxy-piperidin-4-yl group is used as the protecting group. The present invention is particularly applicable to the protection of 2'-hydroxy functions in oligo- or polyribonucleotide synthesis. Compounds comprising hydroxy functions which have been protected by the described groups are also disclosed; as are the necessary reagents and procedures.</p> |
